In-Line Diagnostics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
In-Line Diagnostics Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
In-Line Diagnostics Corp. has 8 FDA 510(k) cleared medical devices. Based in Riverdale, US.
Historical record: 8 cleared submissions from 1995 to 2000. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by In-Line Diagnostics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - In-Line Diagnostics Corp.
8 devices
Cleared
Dec 20, 2000
CRIT-LINE MONITOR III (CLM III)
Gastroenterology & Urology
191d
Cleared
Jul 30, 1999
CRIT-LINE MONITOR III (CLM III)
Gastroenterology & Urology
28d
Cleared
May 27, 1999
CRIT-SCAN II MONITOR
Hematology
230d
Cleared
Oct 09, 1998
MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
Gastroenterology & Urology
88d
Cleared
Dec 11, 1997
CRIT-LINE MONITOR (CLMIII)
Gastroenterology & Urology
163d
Cleared
Jul 23, 1996
CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
Gastroenterology & Urology
391d
Cleared
Mar 14, 1995
CRIT-LINE HEMATOCRIT ALERT
Hematology
27d
Cleared
Jan 19, 1995
CRIT-LINE BLOOD CHAMBER WITH E-BEAM
Gastroenterology & Urology
419d